Associate Technician, Operations

MSD; Wilson (NC); On-site; USD 38,000 - 52,000; Full time

Job summary

MSD in Wilson, NC is hiring a Bio Process Operations Associate Technician for 2nd shift to support aseptic manufacturing on a startup vaccine facility. You will perform primary vaccine filling, inspection, packaging, CIP/SIP, and assist with room and equipment disinfection while maintaining strict GMP compliance.

Candidates should have a high school diploma with 1+ year GMP experience; be able to gown aseptically, wear a respirator if needed, and work with computerized systems.

Qualifications

• One or more years of experience in a GMP manufacturing facility (aseptic GMP environment strongly preferred).
• Ability to gown and work in an aseptic environment.
• Experience working with computerized and automated systems.
• Willing to work irregular hours to support multi-shift operation.
• Excellent communication and teamwork skills.

Responsibilities

• Execute manufacturing operations and facility disinfection per SOPs.
• Perform aseptic vaccine manufacturing steps including filling, inspection, packaging, CIP/SIP.
• Maintain documentation in electronic batch records and logs.
• Adhere to cGMPs and safety procedures; escalate quality or safety issues.
• Support continuous improvement and problem solving with the IPT team.

Skills

Aseptic Handling

Biopharmaceuticals

Chemical Plant Operations

Data Integrity

GMP Awareness

Safety Procedures

Education

High School diploma or equivalent

Tools

SAP

MES

Electronic logbook

Job description

Associate Technician, Operations*This site uses cookies to provide you with an optimal user experience. The cookies include Strictly Necessary and Functional cookies to ensure the site operates as intended (language preference, time zone and workload balance). These cookies are first party cookies, end with the session and are exempted from consent. In addition, this site also uses a Google Analytics Cookie to measure and improve the performance of our site. All information these cookies collect is aggregated and therefore anonymous. By clicking on the ‘Accept Cookies’ button, you are accepting this Performance cookie. You may use this site if you click on the ‘Reject Cookies’ button. To revoke your consent of the Performance cookie, clear your cookies within your browser settings.*### Associate Technician, OperationsApply: Not Applicable: USA - North Carolina - Wilson: Full time: Posted Yesterday: End Date: November 18, 2026 (13 days left to apply): R425412**Job Description**Associate Tech, Operations * Job Description In Primary Posting Language (Include Requirements For Education, Experience And Skills)Bio Process Operations Associate Technician (2nd shift)The Bio Process Operations Technician will be a member of the Maintenance & Operations team within the Vaccines integrated process team for a start-up vaccine manufacturing facility in Wilson, NC. This person is accountable for providing shop floor operations support to aseptic manufacturing within the vaccine manufacturing facility. Tasks will include aseptic primary filling, inspection, packaging, and CIP/SIP. This position will also perform various roles to include executing routine room and equipment disinfection as well as managing the movement of gowning, disinfectants, and materials. In addition to supporting operations activities, the role will be accountable for ensuring that EHS and GMP compliance is maintained within their area of assignment. This position will be an individual contributor and member of the Operations team. **Delivery*** Execute manufacturing operations and facility disinfection* Set up and perform aseptic vaccine manufacturing to include primary filling, inspection, packaging, CIP/SIP, and additional equipment within qualified parameters* Identify potential equipment problems and partner with Vaccines Maintenance Technicians to ensure appropriate resolution. Demonstrate ability to troubleshoot process, electronic systems, and equipment for routine and basic problems.* Perform other duties as requested by the Operations coach **Compliance*** Accountable for performing work in a safe manner, following identified safety procedures (hazardous work permitting, LOTO, HECPs), and using applicable safety equipment / personnel protective equipment (PPE)* Execute operations functions in accordance with current Good Manufacturing Practices (cGMPs) and standard operating procedures (SOPs)* Complete documentation in electronic batch records, electronic logs, and other systems in accordance with site procedure* Maintain good housekeeping and 5S in assigned work area* Adhere to the highest level of data integrity while performing duties* Identify potential quality or safety issues. Escalate as per IPT management processes and assist in the investigation, root cause determination, and CAPA implementation. **Cost*** Ensure that startup activities for area of assignment are executed such that deliverables and timelines are met* Closely monitor team / process performance and improve reliability through problem solving and continuous improvement* Set up and operate equipment in alignment with established training and procedures to ensure reliable operation with minimal delays or discards* Identify and help implement continuous improvement and productivity enhancements within the IPT **Team*** Partner with Technicians and cross-functional groups for assigned area* Demonstrate a high degree of maturity and personal integrity. Strictly adhere to all site policies on personal conduct and attendance.* Train, develop, and mentor other team members to share experience and best practices* Pursue knowledge and skills in assigned area from an operations perspective and share that information readily with team* Maintain a culture of continuous improvement / MPS focused on standard work, making problems visible, minimizing waste, reducing process variability, and problem solving* Routinely demonstrates leadership and conflict-resolution ability. Demonstrates a willingness to provide and receive constructive feedback in 360° performance review. **Reporting Relationships:*** Solid line report to: Manager, Maintenance & Operations* Dotted line report to: N/A* Position(s) reporting to this position: N/A (individual contributor) **Work Schedule:*** 2nd shift 1400 to 2230 **Minimum Education Requirement:*** High School diploma or equivalent **Required Experience and Skills:*** One or more years of experience in a GMP manufacturing facility (aseptic GMP environment strongly preferred).* Demonstrated ability to work independently and as team member* Demonstrated interpersonal skills with ability to influence and assist others through a culture of inclusion, feedback, and empowerment* Ability to gown and work in an aseptic environment* Demonstrated ability to work with computerized and automated systems.* Willing to work irregular hours to support multi-shift operation on an as needed basis* Must be willing and able to wear a respirator for short periods of time, as required, and comply with all respiratory protection program requirements. **Preferred Education, Experience and Skills:*** Associate's degree in business, Science, or Technology-based field and/or bio-pharma focused certificates, such as Bioworks, preferred.* Experience with aseptic filling, visual inspection systems, CIP/SIP systems, packaging equipment and similar aseptic formulation and filling operations* Experience operating, maintaining, troubleshooting, and/or repairing industrial equipment* Experience working in a regulated environment (FDA, etc.) and basic knowledge of cGMPs as they apply to the vaccine/pharmaceutical industry* Experience in Continuous Improvement, Lean Manufacturing, Problem Solving, and/or Right First-Time methodologies* SAP / MES / electronic logbook basic knowledge from a production execution perspective* Demonstrated leadership ability, peer training experience, and/or productivity improvement activities* Demonstrated ability and drive to work autonomously and help organize priorities and work with other team members* Outstanding communication skills both within direct team and across multiple shifts to ensure success of overall team* Ability to support technical writing of documents such as standard operating procedures (SOPs)* Job Description In Secondary Posting Language(s) (Include Requirements For Education, Experience And Skills)* Job Families for Job Profiles #MSJRVETJOBS**Required Skills:**Aseptic Handling, Biopharmaceuticals, Chemical Plant Operations, Computer Literacy, Continuous Improvement Techniques, Data Integrity, Environmental Controls, Good Manufacturing Practices (GMP), Industrial Equipments, Industrial Maintenance, Interpersonal Communication, Manufacturing Operations, Operations Support, Pharmaceutical Production, Pharmaceutical Quality Assurance, Production Scheduling, Productivity Improvements, Safety, Health, Environment and Quality (SHEQ), Safety Procedures, Shift Work, Technology Qualification**Preferred Skills:**Current Employees apply HERECurrent Contingent Workers apply HERE**US and Puerto Rico Residents Only:**Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. 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